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Aripiprazole in Children and Adolescents With Bipolar Disorder and Attention Deficit Hyperactivity Disorder (ADHD)

Aripiprazole in Children and Adolescents With Bipolar Disorder and ADHD: A Randomized Double Blind Placebo Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00116259
Enrollment
50
Registered
2005-06-28
Start date
2005-03-31
Completion date
2008-02-29
Last updated
2008-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit Hyperactivity Disorder, Bipolar Disorder

Keywords

clinical trial, aripiprazole, Bipolar Disorder, Attention-Deficit Hyperactivity Disorder, ADHD

Brief summary

There is a scarcity of clinical trials assessing the effects of medications in children with bipolar disorder. This study aims to assess the efficacy of Aripiprazole (a novel anti-psychotic drug) for the treatment of children and adolescents with bipolar disorder comorbid with ADHD. The study design is a 8-week randomized, double blind, parallel group trial. Patients were randomized to either aripiprazole or placebo. The main hypotheses are: 1. Aripiprazole will significantly reduce maniac scores compared to placebo 2. Aripiprazole will significantly reduce ADHD scores compared to placebo

Detailed description

Bipolar disorder (BD) is a chronic disorder that severely affects the normal development of children and adolescents. The disorder is associated with high rates of suicide tentative and high-risk behaviors like sexual promiscuity and drug abuse. Bipolar disorder in children is also associated with high rates of comorbidity, especially with Attention-Deficit Hyperactivity Disorder (ADHD). There is a scarcity of clinical trials assessing the effects of medications in children with BD. Moreover, the frequent presence of comorbid ADHD might determine lower response to treatment. Aripiprazole is a novel anti-psychotic drug. Its mechanism of action seems to be related to a stabilization of dopaminergic transmission, acting as a partial agonist especially in dopaminergic D2 receptors. It also has effects in 5-HT1a serotonergic receptors. Thus, it might have a promising effect in children and adolescents with comorbid BD and ADHD. A retrospective chart review, recently published, suggests the efficacy of this drug in children with BD. This study aims to assess the efficacy of Aripiprazole (a novel anti-psychotic drug) for the treatment of 50 children and adolescents (age range: 08 to 17 years-old) with Bipolar Disorder comorbid with ADHD. The study design is an 6-week randomized, double blind, parallel group trial. Patients were randomized to either aripiprazole or placebo. The hypotheses are: 1) Aripiprazole will significantly reduce maniac scores compared to placebo; 2)Aripiprazole will significantly reduce ADHD scores compared to placebo; 3) Aripiprazole will not be significantly associated to weight gain compared to placebo.

Interventions

DRUGAripiprazole

Sponsors

Hospital de Clinicas de Porto Alegre
CollaboratorOTHER
Federal University of Rio Grande do Sul
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
8 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Age: 8-17 * BD type I or II comorbid with ADHD * Baseline score in the YMRS \> or = 20

Exclusion criteria

* IQ \< 70 * Pharmacologic treatment in the last month * Pregnancy or absence of a contraceptive method in fertile girls * Diagnoses: pervasive development disorder, schizophrenia, drug abuse or dependency * Risk of suicide or homicide * Clinical condition that might interfere in the study * Known sensibility to aripiprazole

Design outcomes

Primary

MeasureTime frame
Scores in the Young Mania Rating Scale (BD)
Scores in the SNAP-IV (ADHD)
Weight

Secondary

MeasureTime frame
Scores in the Kutcher Adolescent Depression Scale
Scores in the CMRS-P
Report of side events
Scores of quality of life (YQOL-R)
Scores in CGI
Scores in the CDRS

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026